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人类远端结肠顶端膜囊泡中氯离子转运的机制

Mechanism(s) of chloride transport in human distal colonic apical membrane vesicles.

作者信息

Alrefai W A, Ramaswamy K, Dudeja P K

机构信息

Department of Medicine, University of Illinois at Chicago, 60612, USA.

出版信息

Dig Dis Sci. 2001 Oct;46(10):2209-18. doi: 10.1023/a:1011971117097.

Abstract

Previous studies from our laboratory have demonstrated the presence of an electroneutral Cl-/HCO3- exchange process across the human proximal colonic apical membrane vesicles (AMV). However, very little is known about the mechanism(s) of chloride transport in the apical membrane of the human distal colon. Utilizing AMV purified from organ donor distal colonic mucosa and a rapid Millipore filtration technique, the mechanisms of 36Cl- uptake into these vesicles were examined. Outwardly directed OH and HCO3 gradients markedly increased the uptake of 36Cl- into these vesicles, demonstrating a transient accumulation over the equilibrium uptake. Voltage clamping in the presence of K+/valinomycin reduced the OH and HCO3- gradient-stimulated 36Cl- uptake into these vesicles by approximately 30% indicating that the conductive Cl- uptake pathway was present in these vesicles along with the electroneutral exchange process. Under voltage-clamped conditions, the inhibitors the bicarbonate transporters, DIDS and SITS (1 mM), inhibited OH and HCO3- gradient-stimulated 36Cl- uptake by approximately 50%. Acetazolamide showed small but significant inhibition of chloride uptake. Amiloride, bumetanide, and furosemide failed to inhibit 36Cl- uptake. Chloride uptake into these vesicles exhibited saturation kinetics with an apparent Km for chloride of 16.7 mM and a Vmax of 5.9 nmol/mg/15 sec. Chloride, acetate, nitrate, but not sulfate (50 mM each), inhibited 5 mM 36Cl- uptake. Inwardly directed gradients of Na+, K+ or both together did not stimulate chloride uptake into these vesicles indicating that the uptake of Cl- and Na+ in human distal colonic AMV does not involve Na-Cl or Na-K-2Cl cotransport. In conclusion, these studies demonstrate that Cl- transport across the apical membranes of human distal colon involves both conductive pathway and electroneutral Cl-/HCO3- (OH-) exchange processes. In view of our previous demonstration of a Na+/H+ exchange process in these AMV, we propose that the operation of dual ion exchange mechanisms of Na+/H+ and Cl-/HCO3- is the primary mode of electroneutral NaCl absorption across the apical membranes of the enterocytes of the human distal colon.

摘要

我们实验室之前的研究已经证明,在人近端结肠顶端膜囊泡(AMV)中存在一种电中性的Cl⁻/HCO₃⁻交换过程。然而,关于人远端结肠顶端膜中氯离子转运的机制却知之甚少。利用从器官供体远端结肠黏膜纯化得到的AMV和快速的密理博过滤技术,研究了³⁶Cl⁻进入这些囊泡的机制。外向的OH⁻和HCO₃⁻梯度显著增加了³⁶Cl⁻进入这些囊泡的摄取量,表明在平衡摄取量之上有短暂的积累。在存在K⁺/缬氨霉素的情况下进行电压钳制,使OH⁻和HCO₃⁻梯度刺激的³⁶Cl⁻进入这些囊泡的摄取量减少了约30%,这表明在这些囊泡中除了电中性交换过程外,还存在Cl⁻的传导性摄取途径。在电压钳制条件下,碳酸氢盐转运体抑制剂DIDS和SITS(1 mM)使OH⁻和HCO₃⁻梯度刺激的³⁶Cl⁻摄取量减少了约50%。乙酰唑胺对氯离子摄取有轻微但显著的抑制作用。氨氯地平、布美他尼和呋塞米未能抑制³⁶Cl⁻摄取。这些囊泡对氯离子的摄取表现出饱和动力学,氯离子的表观Km为16.7 mM,Vmax为5.9 nmol/mg/15秒。氯离子、乙酸根、硝酸根(各50 mM)能抑制5 mM³⁶Cl⁻的摄取,但硫酸根不能。内向的Na⁺、K⁺梯度或两者共同作用都不能刺激氯离子进入这些囊泡,这表明人远端结肠AMV中Cl⁻和Na⁺的摄取不涉及Na-Cl或Na-K- Cl共转运。总之,这些研究表明,氯离子跨人远端结肠顶端膜的转运涉及传导性途径和电中性的Cl⁻/HCO₃⁻(OH⁻)交换过程。鉴于我们之前在这些AMV中证明了Na⁺/H⁺交换过程,我们提出Na⁺/H⁺和Cl⁻/HCO₃⁻双离子交换机制的运作是氯离子跨人远端结肠肠上皮细胞顶端膜进行电中性吸收的主要模式。

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